Methods and sensors for detection

ABSTRACT

Embodiments of the present disclosure provide for methods of detecting, sensors (e.g., chromogenic sensor), kits, compositions, and the like that related to or use tunable macroporous polymer. In an aspect, tunable macroporous materials as described herein can be used to determine the presence of a certain type(s) and quantity of liquid in a liquid mixture.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is the 35 U.S.C. § 371 national stage of PCTapplication having serial number PCT/US2018/033173, filed on May 17,2018. This application also claims the benefit of and priority to U.S.Provisional Application Ser. No. 62/507,294, having the title “METHODSAND SENSORS FOR DETECTION,” filed on May 17, 2017, the disclosure ofwhich is incorporated herein in by reference in its entirety.

FEDERAL SPONSORSHIP

This invention was made with government support under HDTRA1-15-1-0022awarded by Defense Threat Reduction Agency. The government has certainrights in the invention.

This invention was made with government support under CMMI-1562861awarded by the National Science Foundation. The government has certainrights in the invention.

BACKGROUND

Detection of liquid phase chemical such as ethanol, acetone, andbenzene/toluene/xylene (BTX) requires materials with solvent stabilityand reliability. One of the barriers for sensors is the requirement of asemiconductor device powered by electric current. Hence, there is a needfor a non-semiconductor sensing device.

SUMMARY

Embodiments of the present disclosure provide for methods of detecting,sensors (e.g., chromogenic sensor), kits, compositions, and the likethat related to or use tunable macroporous polymer.

An aspect of the present disclosure provides for a method of measuringthe presence of a first liquid in a liquid mixture, comprising:providing a tunable polymer membrane; and exposing an area of thetunable polymer membrane to a liquid mixture, wherein the area of thetunable polymer membrane exposed to the liquid mixture changes color ifthe liquid mixture includes a first liquid.

An aspect of the present disclosure provides for a chromogenic sensor,comprising: a tunable polymer membrane, wherein an area of the tunablepolymer membrane has the characteristic of changing color upon exposureto a first liquid if the first liquid is present in a liquid mixture.

An aspect of the present disclosure provides for a kit for testing thepresence of a first liquid, comprising: a chromogenic sensor comprisinga tunable polymer membrane, wherein an area of the tunable polymermembrane has the characteristic of changing color upon exposure to afirst liquid if the first liquid is present in a liquid mixture;instructions for use of the chromogenic sensor to test for the presenceof the first liquid in a liquid mixture.

An aspect of the present disclosure provides for a method of making aphotonic structure, comprising: disposing nanoparticles onto a surfaceto form a three dimensional array of particles; introducing a prepolymermixture to the array of particles; polymerizing the prepolymer mixtureto form a polymer framework around the three dimensional array ofparticles; and removing the particles to form a three dimensional arrayof macropores to form a macroporous photonic crystal membrane, whereinthe three dimensional polymer framework separates the macropores.

An aspect of the present disclosure provides for a tunable polymermembrane fabricated by the method described above and herein.

Other structures, kits, methods, features, and advantages will be orbecome apparent to one with skill in the art upon examination of thefollowing drawings and detailed description. It is intended that allsuch additional structures, kits, methods, features and advantages beincluded within this description, be within the scope of the presentdisclosure, and be protected by the accompanying claims.

BRIEF DESCRIPTION OF THE DRAWINGS

Many aspects of the disclosed devices and methods can be betterunderstood with reference to the following drawings. The components inthe drawings are not necessarily to scale, emphasis instead being placedupon clearly illustrating the relevant principles. Moreover, in thedrawings, like reference numerals designate corresponding partsthroughout the several views.

FIG. 1 illustrates an embodiment of a method for fabricating macroporouspolymer membranes using a silica nanoparticle-based photonic crystal.

FIG. 2 illustrates a second embodiment of a method for fabricatingmacroporous polymer membranes using a silica nanoparticle-based photoniccrystal.

FIG. 3 illustrates a third embodiment of a method for fabricatingmacroporous polymer membranes using a silica photonic crystal template.

FIG. 4 illustrates a fourth embodiment of a method for fabricatingmacroporous polymer membranes using a silica multilayers or singletemplate.

FIG. 5A is a photograph showing an example of the silica coating methoddescribed herein.

FIG. 5B depicts a photograph of a polyurethane membrane templated fromFIG. 5A.

FIG. 6 illustrates normal-incidence transmission spectra obtained fromthe macroporous polymer film with different drying rates.

FIG. 7 illustrates a photograph of a macroporous polymer film dipping ina commercial ethanol-free fuel (TruFuel®) blended with 2% of ethanol.Polymer film with deformation at the center before (A) and after (B).Scale bar: 5 mm.

FIGS. 8A-C illustrate typical SEM images of (FIG. 8A) Cross-section viewof a greenish area from a macroporous polymer film. (FIG. 8B)Cross-section view of a deformed area. (FIG. 8C) Cross-sectional view ofa recovered area.

FIG. 9 illustrates an image of chromogenic sensor for ethanol sensing.

FIG. 10 illustrates specular optical reflection spectra for detectingdifferent concentrations of ethanol blended with octane.

FIG. 11 illustrates specular optical reflection spectra for detectingtrace amount of ethanol blended with octane.

FIG. 12 illustrates specular optical reflection spectra for detectingethanol vapor above ethanol-octane mixtures with different ethanolconcentrations.

FIG. 13 illustrates a linear relationship between the positions of theoptical reflection peaks and the ethanol concentrations inethanol-octane mixtures.

FIGS. 14A-D illustrate specular optical reflection spectra for detectingethanol in ethanol-free TruFuel®, Shell® gasoline, NyQuil™ medicine, andmouthwash liquids.

FIG. 15 illustrates schematics of smartphone-based sensor analysisprocedure.

FIG. 16 illustrates a database of smartphone analysis to compare RGBdata to ethanol concentration.

DETAILED DESCRIPTION

Before the present disclosure is described in greater detail, it is tobe understood that this disclosure is not limited to particularembodiments described, as such may, of course, vary. It is also to beunderstood that the terminology used herein is for the purpose ofdescribing particular embodiments only, and is not intended to belimiting, since the scope of the present disclosure will be limited onlyby the appended claims.

Where a range of values is provided, it is understood that eachintervening value, to the tenth of the unit of the lower limit (unlessthe context clearly dictates otherwise), between the upper and lowerlimit of that range, and any other stated or intervening value in thatstated range, is encompassed within the disclosure. The upper and lowerlimits of these smaller ranges may independently be included in thesmaller ranges and are also encompassed within the disclosure, subjectto any specifically excluded limit in the stated range. Where the statedrange includes one or both of the limits, ranges excluding either orboth of those included limits are also included in the disclosure.

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this disclosure belongs. Although any methods andmaterials similar or equivalent to those described herein can also beused in the practice or testing of the present disclosure, the preferredmethods and materials are now described.

As will be apparent to those of skill in the art upon reading thisdisclosure, each of the individual embodiments described and illustratedherein has discrete components and features which may be readilyseparated from or combined with the features of any of the other severalembodiments without departing from the scope or spirit of the presentdisclosure. Any recited method can be carried out in the order of eventsrecited or in any other order that is logically possible.

Embodiments of the present disclosure will employ, unless otherwiseindicated, techniques of chemistry, inorganic chemistry, materialscience, and the like, which are within the skill of the art. Suchtechniques are explained fully in the literature.

The following examples are put forth so as to provide those of ordinaryskill in the art with a complete disclosure and description of how toperform the methods and use the compositions and compounds disclosed andclaimed herein. Efforts have been made to ensure accuracy with respectto numbers (e.g., amounts, temperature, etc.), but some errors anddeviations should be accounted for. Unless indicated otherwise, partsare parts by weight, temperature is in ° C., and pressure is inatmosphere. Standard temperature and pressure are defined as 25° C. and1 atmosphere.

Before the embodiments of the present disclosure are described indetail, it is to be understood that, unless otherwise indicated, thepresent disclosure is not limited to particular materials, reagents,reaction materials, manufacturing processes, or the like, as such canvary. It is also to be understood that the terminology used herein isfor purposes of describing particular embodiments only, and is notintended to be limiting. It is also possible in the present disclosurethat steps can be executed in different sequence where this is logicallypossible.

It must be noted that, as used in the specification and the appendedclaims, the singular forms “a,” “an,” and “the” include plural referentsunless the context clearly dictates otherwise. Thus, for example,reference to “a support” includes a plurality of supports. In thisspecification and in the claims that follow, reference will be made to anumber of terms that shall be defined to have the following meaningsunless a contrary intention is apparent.

DISCUSSION

Embodiments of the present disclosure provide for methods of detecting,sensors (e.g., chromogenic sensor), kits, compositions, and the likethat related to or use tunable macroporous polymer. In an aspect,tunable macroporous materials as described herein can be used todetermine the presence of a certain type(s) and quantity of liquid in aliquid mixture. Embodiments of the present disclosure are simple to use,provide robust results, and are re-useable while also being inexpensive.

In an aspect, the present disclosure provides for a unique macroporousstructure that can be made by a simple and scalable nanoparticleself-assembly technology. This technology can result in unusual “cold”programming and subsequent room-temperature recovery, which can becycled, for a large variety of polymers. The tunable properties aredescribed herein. The flexibility of the methods and compositionsdescribed herein could expand and simplify the application scopes ofnew, tunable, materials that can be used as sensors or in methods ofdetecting the presence of and/or concentration of a liquid in a liquidmixture.

In an aspect, the present disclosure includes a method of measuring thepresence and/or concentration of a first liquid (or multiple differenttypes of liquids) in a liquid mixture. The liquid mixture (e.g., anaqueous or non-aqueous mixture) can optionally include a first liquid(e.g., an organic solvent). The tunable polymer membrane can be exposedto the liquid mixture in one or more ways. In an aspect, the tunablepolymer membrane or a portion thereof can be dipped into the liquidmixture. In another aspect, an amount (e.g., a drop or larger amount) ofthe liquid mixture can be disposed onto the surface of the tunablepolymer membrane. In an aspect, an area of the tunable polymer membranecan be exposed to the vapor of the liquid mixture. In an aspect, thetunable polymer membrane or a portion of thereof can be dipped into theliquid mixture.

Upon exposure of the tunable polymer membrane to the liquid mixture, thetunable polymer membrane can change color, for example from a greenishcolor to a bluish color, yellowish color, or orange color, dependingupon the concentration of the first liquid in the liquid mixture (SeeExample 1). The color and color change can be tuned based on thecomposition of the tunable polymer membrane and/or the method of makingthe tunable polymer membrane. In an aspect, the color change isdetectable. In one aspect, the color change is perceptible by the humaneye for those that can perceive the particular colors of the colorchange. It is understood that some individuals have degrees of colorblindness, so the color change may not be perceived by thoseindividuals. In another aspect, the color change can be evaluated usingan analysis system to measure the color change from before to after orjust after the change and correlate the color change using a knownstandard to the identity of the first liquid and/or the concentration ofthe first liquid. In an aspect, the analysis system can include a mobiledevice such as a cell phone, tablet, or laptop, where a picture or imagecan be captured and subsequently be analyzed.

In an embodiment, the tunable polymer membrane can be used in achromogenic sensor and kit to determine the presence of and/orconcentration of a first fluid in the liquid mixture (e.g., the liquidform, the vapor form, or both). For example, the method, chromogenicsensor, or kit can be useful for detecting the presence or concentrationof a component in fuel. In an embodiment, the first liquid can be anorganic solvent that can interact with the polymer such as an alcohol(e.g., ethanol) and the liquid mixture can be an aqueous mixture or anon-aqueous mixture such as a hydrocarbon mixture like gasoline. In thisregard, the method, chromogenic sensor, or kit of the present disclosurecan be used to measure the amount of ethanol in the gasoline, which canbe useful in situations that require low or zero ethanol in thegasoline, such as in aircraft fuel.

In regard to the kit, the kit would have instructions and optionally awipe(s) to clean off the surface of the tunable polymer membrane,gloves, a device to expose the liquid mixture to the tunable polymermembrane, and the like. The instructions would, among other things,provide guidance on how to perform the test, evaluate the test (e.g.,guide for what the color change means (e.g., presence of a first liquid,concentration of the liquid, or the like)), clean the tunable polymermembrane, use the analysis system (e.g., use the mobile device, thewebpage to evaluate the results, and the like). The instructions mayinclude other guidance as well to evaluate the contents of the liquidmixture in question.

Now having described the method, sensor, and kit, additional detailswill be provided that describe methods for preparing tunable materials.FIGS. 1-3 are flowcharts depicting embodiments of methods describedherein. FIG. 4 shows a further embodiment of a method for fabricatingmacroporous polymer membranes using a silica photonic crystal template

In an embodiment, the colloidal crystal of silica particles can beformed by first synthesis of silica particle. Monodispersed silicaparticles (e.g., microspheres), with longest dimension (e.g., a diameterfor a spherical particle) of about 100 to 10,000 nm, were synthesized bythe standard Stöber method or other appropriate method. Silica particleswere self-assembled on a substrate such as a glass microslide, which isplaced in a clean scintillation vial including about 15 ml of ethanolwith 1 vol % of silica particles, by the convective self-assemblytechnology to form colloidal crystals. Other monodispersed particles,such as polystyrene and poly(methyl methacrylate) (PMMA) particles, canalso be used in assembling colloidal crystals using the convectiveself-assembly technology. These polymer latex particles can beselectively removed in organic solvents, such as toluene or acetone.

In an embodiment, a convective self-assembly method can enable theformation of ordered colloidal silica crystals on a glass substrate.Silica particles with a diameter of about 100 to 10,000 nm, which can bedispersed in an alcohol such as ethanol, can be assembled on the glassslides. The substrate can be varied in size depending of the desiredapplications.

After the silica layer or multilayer is applied, a polymer castingapparatus can be assembled. One or more substrates can be coated with alayer of silica particles as described above. In an embodiment, two ormore substrates or a surface of two or more substrates can be coatedwith a silica layer. In an embodiment of a polymer casting apparatus,two or more coated substrates can be positioned in a containerconfigured to hold a solvent in a sandwich-type configuration so that atleast a surface of a first substrate coated with silica opposes asurface of a second substrate, uncoated or coated with silica. Otherconfigurations can be realized with more than two coated substrates. Inan embodiment, the coated substrates of the polymer casting apparatusare silica-coated glass.

In an embodiment, after assembly of the polymer casting apparatus,monomers or a monomer composition can be put in a space between two ormore opposing silica coated surfaces of the two or more silica coatedsubstrates. Monomers or a monomer composition that can form a polymer, adesired polymer, or a pre-determined polymer are described in moredetail below.

After monomers are placed in the space, they can be polymerized by apolymerization method to form a tunable polymer membrane. Thepolymerization method can be photo-polymerization, wherein the monomersare polymerized by the application of light. In an embodiment, the lightcan be UV light and can be applied for a period of time.

The tunable polymer membrane can be made of a monomer, a monomercomposition, or a polymer. In some embodiments, the monomers, monomercomposition, or polymer can be a viscous and/or elastic polymer. Thetunable polymer membrane can additionally be characterized by weakintermolecular forces. Further, the tunable polymer membrane can have ahigh Young's modulus and can still be reconfigurable via coldprogramming.

Following polymerization, the silica layers can be removed from themembrane and the membrane optionally washed. In an embodiment, thesilica layer is removed by a solvent. In an embodiment, the silica isremoved by 2% hydrofluoric acid (HF) aqueous solution. In an embodiment,the membrane can be washed by a wash solvent. In an embodiment, the washsolvent can be deionized water. The silica layers can be removed by asolvent that is placed in the container of the polymer casting apparatusin an embodiment. Selective removal of the silica layers can createmacropores in the polymer. The polymer or tunable polymer membrane canbe macroporous following removal of the templating silica layer.

In an embodiment, after removal of the silica monolayer (and optionalwash), the polymer casting apparatus can be disassembled and the polymermembrane separated from the substrates that were previously silicacoated. In an embodiment, the polymer membrane can be a tunablemembrane.

The tunable polymer membrane can be configured to be modified such thatthe color of the tunable polymer membrane can vary in response to one ormore liquids to which the tunable polymer membrane is exposed. The slowdrying of liquid can cause a deformation of the tunable polymer membranethat changes the shape or configuration of the macropores in the tunablepolymer membrane.

The color characteristics of the tunable membrane can be altered bydrying after application of or cold programming. A solvent can alter thetransparency by changing the shape of the macropores in the tunablepolymer membrane through a mechanism such as capillary action.

The color change of the tunable polymer membrane can be cycled, or inother words is reversible. The color of the tunable polymer membrane asdescribed herein can changed by exposure to a liquid mixture (e.g.,ethanol in gasoline) and then returned to the original color by coldprogramming.

The methods and compositions described herein can use a large variety ofshape memory polymers to form the tunable polymer membrane depending onthe desired configuration of the tunable polymer membrane. Shape memorypolymers (SMP) as described herein can be elastic or glassy.

A “glassy” polymer can be a polymer or copolymer with glass transitiontemperature higher than room temperature. A “glassy” polymer can beoptically transparent. A glassy polymer as used herein can have a glasstransition state (T_(g)) higher than room temperature. In an embodiment,a glassy polymer has a T_(g) of about 120° C. In an embodiment, theglassy polymer is poly(urethane) (with a typical T_(g) of about 90° C.),polyethylene terephthalate (PET) and polyethyleneoxide (PEO), epoxy,polyarylates, block copolymers containing polystyrene andpoly(1,4-butadiene), and poly(2-methyl-2-oxazoline) andpolytetrahydrofuran, polynorbornene, and other types of shape memorypolymers.

In an embodiment, a polymer or tunable polymer membrane as used hereincan be polymerized poly(urethane). In an embodiment, a polymer as usedherein is a glassy membrane comprising poly(urethane)s. A coating asdescribed herein can be a glassy membrane. A coating as described hereincan be a glassy membrane comprising poly(urethane)s. In an embodiment, aglassy polymer can be used to form a membrane. In an embodiment,poly(urethane)s can be used to form a membrane.

A silica nanoparticle monolayer can be used as a structural template forfabricating macroporous polymer membranes. The templating layer can bemultilayers of silica nanoparticles assembled by various methodologies,such as spin coating, dip coating, doctor blade coating, and so on. Inan embodiment, the silica nanoparticles can be self-assembled or not beself-assembled and/or possess long-range ordering or not possesslong-range ordering. Self-assembled silica nanoparticle monolayers canbe used as described herein and can be created by a variety of methods,for example a simple and scalable Langmuir-Blodgett method as describedabove. As used and described herein, silica nanoparticles can be usedfor silica nanoparticle monolayers or multilayers. Silica nanoparticlescan be Si_(x)O_(y)H_(z), synthesized by various methodologies, includingthe well-established Stöber method.

In an embodiment, the silica nanoparticles can be about 100 nm to about10,000 nm. In an embodiment, silica nanoparticles are silicon dioxide(SiO₂). In an embodiment, a composition of silica nanoparticles has anaverage diameter of about 350 nm/particle. Silica nanoparticles as usedherein can have a diameter of about 350 nm. In an embodiment, silicananoparticles as used herein can be SiO₂ nanoparticles with a diameterof about 350 nm each.

EXAMPLES

Now having described the embodiments of the disclosure, in general, theexamples describe some additional embodiments. While embodiments of thepresent disclosure are described in connection with the example and thecorresponding text and figures, there is no intent to limit embodimentsof the disclosure to these descriptions. On the contrary, the intent isto cover all alternatives, modifications, and equivalents includedwithin the spirit and scope of embodiments of the present disclosure.

Example 1

In this disclosure, a templating fabricated macroporous polymer photoniccrystal that responds to selected compounds can be used as a chemicalsensor with fast response and high sensitivity. The system isspecifically designed to detect the presence and even measuring thetarget chemical in a multicomponent solution (ethanol in gasoline). Thedetection could be done by dipping the sensor in the liquid mixture aswell as placing the sensor above the solution surface, which depends onthe detection limit. The selective-interaction of a target compoundswith the sensor provides a unique capability for chemical detection.

Silica particles were self-assembled on a glass microslide by theconvective self-assembly technology to form colloidal crystals. Variousthickness of resulting colloidal crystals (10-50 layers) were observedas a result of different particle volume fraction of the silicamicrospheres/ethanol suspension. The microslide with silica colloidalcrystal was then allowed to stick to a blank microslide with a ˜1 mmthick spacer in between. Next, a viscous oligomer mixture (CN945A70,Sartomer) consisting of trifunctional acrylated urethane, tripropyleneglycol diacrylate (TPGDA), and photoinitiator (Darocur 1173,2-hydroxy-2-methyl-1-phenyl-1-propanone, BASF) was preheated to 90° C.and then transferred into the space between the microslides. Thecapillary force assisted the infiltration of the oligomer mixture intothe interstitial of silica microspheres and was evident as the oligomermixture and silica particle index-matched and the sample cell turnedtransparent. The sample was then polymerized using a pulsed UV curingsystem (RC 742, Xenon) for 4 s. Last, the polymerized sample was removedfrom the glass microslide and subsequently soaked in a 1 vol %hydrofluoric acid aqueous solution for 24 h. The etched sample wasrinsed with deionized water, ethanol and dried in air. The final productis in greenish diffractive color when observed at large viewingangles)(>45°.

Cold programming experiments on the free-standing macroporous polymerfilm were performed where organic solvent (e.g., acetone andacetonitrile) was added dropwise on the film surface. Greenishdiffractive color remained when the solvent was removed within 5 secondsusing Kimwipes™ or air dry (FIG. 6. blue-peak). The original diffractivecolors were changed/lost after we leave the solvent on the surface anddried naturally in ˜2 min (FIG. 6 orange-peak).

The bluish-iridescent color of the deformed areas is caused by the Braggdiffraction of visible light from the deformed macroporous film (seeFIG. 7B). FIG. 8A shows the top-view SEM image of the greenish originalarea from the macroporous polymer film. FIG. 8B is the cross-sectionalSEM image of a bluish deformed area of the macroporous polymer film. Therecovered of the macroporous 3-D order is shown by the cross-sectionalSEM image in FIG. 8C.

We utilized this unique cold programming cycle (deform and thenrecovery) with all-room-temperature-approach to design a chromogenicsensor, which uses the degree of recovery as a sensing parameter. Achromogenic sensor was fabricated to demonstrate the visible colorchange when in contact with different concentration of the analyte,which is ethanol in this case. In FIG. 9, the sample changed fromtransparent to blue, yellow, then orange, when exposed to differentconcentrations of ethanol in gasoline (0 ppm, 2000 ppm, 3000 ppm, 4000ppm, 5000 ppm, 6000 ppm, respectively). Furthermore, the response timeof the chromogenic sensor was less than ˜3 seconds.

The ethanol in gasoline (mostly alkanes) swells the SMP chromogenicsensor, and the degree of swelling is higher when the concentration ofethanol is greater. To further study the precise effect of swelling andethanol concentration, we utilized a two-component system—ethanol inoctane. By using a vis-NIR spectrometer, we could obtain a concentrationdependence spectra due to the light diffraction of SMP with a responsetime of 5 s. The SMP begins at fully deformed state and then graduallyrecovers with increasing ethanol concentration. The SMP is fullyrecovered when the ethanol concentration is at 5500 ppm (FIG. 10).

To further explore the sensitivity at low concentration, we experimentthe SMP by allowing the sensor to response for 8 h under extremely lowethanol concentrations (FIG. 11). The optical spectra show a distinctdiffraction response for ethanol concentration as low as 10 ppm, magentacurve.

Low concentration aside, our chromogenic sensor could also detectethanol at relatively high concentration. The idea is to distinguishethanol concentration in gasoline by using its relative vapor pressure.FIG. 12 shows the reflection spectra of the SMP when sensing the vaporof various gasoline with ethanol content ranging from 5-30 vol %. TheSMP had a gradual red shift as the concentration of ethanol, hence thevapor pressure of ethanol, increased from 5% to 30%. FIG. 13 illustratesan optical characterization of ethanol sensor with ethanol vapor whenthe concentration increases from 5 to 30 vol %.

Moreover, sensing experiments were performed using commercial products.The deformed polymer was used to test commercial product with ethanoland its control product that is ethanol-free. First, we investigate oursensor performance for gasoline. We first test the sensor with TruFuel®,which is a commercially sold ethanol free gasoline with 92 octanenumber. The optical spectra show both flat curve in grey color (FIGS.14A-D). Then, the sensors were separately deformed and triggered byusing TruFuel® with 1% of ethanol added and Shell® gasoline in liquidand vapor respectively. Both shows orange iridescent peak ˜630 nm(yellow and orange peak in FIGS. 14A and 14B, respectively). We thencarried out a test for various pharmaceutical products. The chromogenicsensor shows no color change when triggered by ethanol free Nyquil™.Whereas the sample triggered with regular Nyquil™ shows significantcolor change (dark blue peak in FIG. 14C). The same result is presentedwhen the sensor use to distinguish daily supplies such as mouthwash. Thesensor could differentiate commercially sold ethanol free Listerine toregular ones (FIG. 14D).

Lastly, we developed a chromogenic sensor analysis tool usingsmartphones (FIG. 15). We generated an RGB calorimetric profile databaseof the SMP sensor when exposed to ethanol with known concentration (FIG.16). When a customer captured a new image for analysis, its RGB datawill show in the app, and the results could be looked up in the databasefor analysis. We believe our unique SMP-based sensor and instantanalysis system can be easily extended to the analysis of many moretarget chemicals in the desired system.

Ratios, concentrations, amounts, and other numerical data may beexpressed in a range format. It is to be understood that such a rangeformat is used for convenience and brevity, and should be interpreted ina flexible manner to include not only the numerical values explicitlyrecited as the limits of the range, but also to include all theindividual numerical values or sub-ranges encompassed within that rangeas if each numerical value and sub-range is explicitly recited. Toillustrate, a concentration range of “about 0.1% to about 5%” should beinterpreted to include not only the explicitly recited concentration ofabout 0.1% to about 5%, but also include individual concentrations(e.g., 1%, 2%, 3%, and 4%) and the sub-ranges (e.g., 0.5%, 1.1%, 2.2%,3.3%, and 4.4%) within the indicated range. In an embodiment, the term“about” can include traditional rounding according to significant figureof the numerical value. In addition, the phrase “about ‘x’ to ‘y’”includes “about ‘x’ to about ‘y’”.

Unless defined otherwise, all technical and scientific terms used havethe same meaning as commonly understood by one of ordinary skill in theart to which this disclosure belongs. Although any methods and materialssimilar or equivalent to those described can also be used in thepractice or testing of the present disclosure, the preferred methods andmaterials are now described.

Embodiments of the present disclosure will employ, unless otherwiseindicated, techniques of separating, testing, and constructingmaterials, which are within the skill of the art. Such techniques areexplained fully in the literature.

It should be emphasized that the above-described embodiments are merelyexamples of possible implementations. Many variations and modificationsmay be made to the above-described embodiments without departing fromthe principles of the present disclosure. All such modifications andvariations are intended to be included herein within the scope of thisdisclosure and protected by the following claims.

The invention claimed is:
 1. A method of measuring the presence of afirst liquid in a liquid mixture, comprising: providing a tunable shapememory polymer membrane wherein the tunable shape memory polymermembrane is an optically transparent glassy polymer having a glasstransition temperature higher than room temperature, wherein the glassypolymer is selected from poly(urethane), polyethylene terephthalate(PET), polyethyleneoxide (PEO), epoxy, polyarylates, block copolymerscontaining polystyrene and poly(1,4-butadiene),poly(2-methyl-2-oxazoline), and polytetrahydrofuran, and polynorbornene,wherein the tunable shape memory polymer membrane is a macroporousphotonic crystal membrane having a three-dimensional polymer frameworkseparating macropores; and exposing an area of the tunable shape memorypolymer membrane to the liquid mixture, wherein the area of the tunableshape memory polymer membrane exposed to the liquid mixture changescolor if the liquid mixture includes the first liquid; wherein the colorchange is correlated to a concentration of the first liquid in theliquid mixture or pressure of vapor of the first liquid in the liquidmixture; wherein the area changes color depending upon the concentrationof the first liquid in the liquid mixture, wherein the color changesfrom a greenish color to a bluish color in response to a firstconcentration, yellowish color in response to a second concentration,and orange color in response to a third concentration, and wherein thefirst concentration, the second concentration, and the thirdconcentration are different from one another.
 2. The method of claim 1,wherein the color change is detectable.
 3. The method of claim 1,wherein the first liquid is an organic solvent.
 4. The method of claim3, wherein the organic solvent is ethanol.
 5. The method of claim 4,wherein the liquid mixture is gasoline.
 6. A method of measuring thepresence of an organic solvent in gasoline, comprising: providing atunable shape memory polymer membrane wherein the tunable shape memorypolymer membrane is an optically transparent glassy polymer having aglass transition temperature higher than room temperature, wherein thetunable shape memory polymer membrane is a macroporous photonic crystalmembrane having a three-dimensional polymer framework separatingmacropores; and exposing an area of the tunable shape memory polymermembrane to the gasoline, wherein the area of the tunable shape memorypolymer membrane exposed to the gasoline changes color if the liquidmixture includes the organic solvent; wherein the color change iscorrelated to a concentration of the organic solvent in the gasoline orpressure of vapor of the organic solvent in the gasoline; wherein theorganic solvent is ethanol, and wherein the area changes color dependingupon the concentration of organic solvent in the gasoline, wherein thecolor changes from a greenish color to a bluish color in response to afirst concentration, yellowish color in response to a secondconcentration, and orange color in response to a third concentration,and wherein the first concentration, the second concentration, and thethird concentration are different from one another.